Welcome Guest
Log In
|
Sign Up
Transport of inorganic cations/anions and amino acids/oligopeptides
SuperPath
Pathway network
for
Transport of inorganic cations/anions and amino acids/oligopeptides
SuperPath
45
Pathways
in the
Transport of inorganic cations/anions and amino acids/oligopeptides
SuperPath
Defective SLC16A1 causes symptomatic deficiency in lactate transport (SDLT)
Sodium/Proton exchangers
Transport of small molecules
Defective SLC24A5 causes oculocutaneous albinism 6 (OCA6)
Defective SLC20A2 causes idiopathic basal ganglia calcification 1 (IBGC1)
SLC-mediated transmembrane transport
Defective SLC22A5 causes systemic primary carnitine deficiency (CDSP)
Defective SLC34A1 causes hypophosphatemic nephrolithiasis/osteoporosis 1 (NPHLOP1)
Sodium-coupled phosphate cotransporters
Transport of bile salts and organic acids, metal ions and amine compounds
Defective SLC12A1 causes Bartter syndrome 1 (BS1)
Defective SLC34A3 causes Hereditary hypophosphatemic rickets with hypercalciuria (HHRH)
Organic anion transporters
Organic anion transport
Cation-coupled Chloride cotransporters
Defective SLC22A12 causes renal hypouricemia 1 (RHUC1)
Variant SLC6A14 may confer susceptibility towards obesity
Defective SLC9A6 causes X-linked, syndromic mental retardation,, Christianson type (MRXSCH)
Bicarbonate transporters
Defective SLC17A5 causes Salla disease (SD) and ISSD
Defective SLC36A2 causes iminoglycinuria (IG) and hyperglycinuria (HG)
Amino acid transport across the plasma membrane
Defective SLC22A18 causes lung cancer (LNCR) and embryonal rhabdomyosarcoma 1 (RMSE1)
Defective RHAG causes regulator type Rh-null hemolytic anemia (RHN)
Defective SLC24A4 causes hypomineralized amelogenesis imperfecta (AI)
Defective SLC17A8 causes autosomal dominant deafness 25 (DFNA25)
Proton-coupled neutral amino acid transporters
Rhesus glycoproteins mediate ammonium transport.
Defective SLC26A3 causes congenital secretory chloride diarrhea 1 (DIAR1)
Sodium/Calcium exchangers
Sodium-coupled sulphate, di- and tri-carboxylate transporters
Multifunctional anion exchangers
Proton/oligopeptide cotransporters
Defective SLC26A4 causes Pendred syndrome (PDS)
Transport of inorganic cations/anions and amino acids/oligopeptides
Na+/Cl- dependent neurotransmitter transporters
Inositol transporters
Defective SLC4A4 causes renal tubular acidosis, proximal, with ocular abnormalities and mental retardation (pRTA-OA)
Defective SLC9A9 causes autism 16 (AUTS16)
Proton-coupled monocarboxylate transport
Organic cation/anion/zwitterion transport
Defective SLC12A6 causes agenesis of the corpus callosum, with peripheral neuropathy (ACCPN)
Organic cation transport
Defective SLC12A3 causes Gitelman syndrome (GS)
Type II Na+/Pi cotransporters
728
Genes
in the
Transport of inorganic cations/anions and amino acids/oligopeptides
SuperPath
SLC6A14
SLC22A12
SLC34A3
SLC36A2
SLC6A19
SLC6A18
SLC22A18
SLC6A20
SLC6A15
SLC6A6
SLC6A12
SLC34A1
SLC22A1
SLC22A2
SLC22A5
SLC16A1
BSG
SLC9A6
SLC9A9
SLC34A2
SLC22A7
SLC24A4
SLC26A3
SLC36A1
SLC17A8
SLC17A5
SLC24A5
SLC26A4
SLC22A15
SLC22A11
RHAG
RSC1A1
SLC12A1
SLC12A3
SLC20A2
SLC22A3
SLC22A4
SLC22A16
RUNX1
SLC4A4
SLC22A6
SLC22A8
SLC12A6
SLC9A8
SLC9A4
SLC9A1
SLC9A2
SLC9A3
SLC9A5
SLC9A7
SLC12A7
SLC26A1
SLC38A3
SLC7A9
SLC2A13
SLC26A9
SLC26A7
SLC5A11
SLC16A10
SLC36A4
SLC15A4
SLC25A29
SLC43A2
EMB
SLC25A10
SLC5A12
SLC5A8
SLC26A2
AHCYL2
SLC7A8
SLC16A8
SLC7A11
SLC24A2
SLC13A4
SLC13A5
SLC26A11
SLC15A3
RHCG
SLC38A2
SLC38A4
SLC7A10
SLC17A7
SLC17A6
RHBG
SLC4A10
SLC24A3
SLC12A5
SLC4A5
SLC13A3
SLC26A6
SLC4A3
SLC1A4
SLC1A5
SLC3A1
SLC3A2
SLC4A1
SLC4A2
SLC5A5
SLC6A1
SLC6A2
SLC6A3
SLC6A7
SLC6A9
SLC6A11
SLC6A13
SLC7A1
SLC7A2
SLC8A2
SLC8A1
SLC8A3
SLC12A2
SLC12A4
SLC13A1
SLC15A1
SLC15A2
SLC17A1
SLC18A1
SLC18A2
SLC20A1
SRI
SLC25A22
SLC8B1
CALM1
CALM2
CALM3
SLC7A5
SLC38A1
SLC4A9
SLC25A18
SLC7A3
SLC43A1
SLC7A7
SLC7A6
SLC13A2
SLC16A3
SLC6A5
SLC24A1
SLC16A7
SLC38A5
SLC4A7
SLC4A8
SLC25A26
SLC44A3
SLC31A1
CP
SLC32A1
SLC47A2
CTNS
SLC30A8
SLC44A5
SLC44A1
SLC39A14
SLC41A1
SLC39A6
SLC39A1
SLC39A5
SLC39A3
SLC39A2
SLC40A1
SLC10A6
SLC11A2
SLC47A1
SLC30A10
SLC39A4
SLC44A2
SLC39A10
SLC5A7
SLC39A8
SLC30A5
SLC1A1
SLC1A2
SLC1A3
SLC1A6
SLC1A7
SLC11A1
SLC14A1
SLC30A1
SLC30A2
SLC30A3
SLC39A7
SLC44A4
SLC14A2
SLC41A2
HEPH
SLC35A1
SLCO1B1
SLC27A4
SLC35D2
SLC2A6
SLCO2B1
SLC5A10
SLC2A14
SLC2A12
SLC2A7
SLC5A9
SLC29A1
SLC29A4
SLC35D1
SLC35A3
ARL2BP
FGF21
SLCO4A1
SLCO3A1
SLCO1B3
LCN12
SLC27A6
SLC25A4
SLC25A5
SLC25A6
SLC2A8
SLC29A2
APOD
SLC35B2
SLCO4C1
SLC27A1
LCN15
LCN9
LCN1
ARL2
SLC35B3
PDZD11
SLCO1C1
AVP
SLC29A3
SLC35C1
SLC50A1
SLC2A9
SLC28A3
SLC2A1
SLC2A2
SLC2A3
SLC2A4
SLC5A1
SLC5A2
SLC5A4
SLC16A2
SLCO2A1
SLCO1A2
SLC2A11
SLC35A2
SLC2A10
SLC35B4
SLC45A3
SLC5A6
SLC28A2
SLC28A1
MFSD4B
SLC33A1
C8orf44-SGK3
ABCC5
ABCB6
ABCC9
NR1H3
ATP9A
SGK2
PSME3
PSMD14
ABCC4
TCIRG1
TRDN
ABCA7
ABCA10
ABCA9
ABCA8
MICU1
ATP8A1
GLRX3
NPC2
ERLIN1
GNB5
ADCY1
CETP
YME1L1
SLC17A3
ADCY2
CFTR
ADCY3
AFG3L2
OS9
RIPK3
WWP1
ADCY5
ERLIN2
ABCB8
ADCY6
ADCY7
SLC46A1
PHB2
ADCY8
CYGB
ADCY9
APOA5
AP2M1
AP2S1
CLCA1
ADD1
CLCN1
CLCN2
CLCN3
CLCN4
CLCN5
CLCN6
CLCN7
CLCNKA
CLCNKB
ADD2
CLIC2
ADD3
CLTA
CLTC
ANO4
PSMB11
NIPA1
ABCC2
ATP6V1G3
SLC9B2
TRPM6
PSMA8
BEST3
CSN1S1
CSN3
ATP8B3
SLC9B1
NIPAL1
ATP6V0E2
AP2A1
AP2A2
STOML3
TRPV3
AP2B1
TSC22D3
ABCA1
EIF2S1
ANO6
EIF2S3
ADCY4
MLKL
A2M
ABCA2
ANO5
DMTN
STOM
ABCA3
ALB
ABCD1
TPCN2
ABCB7
MICU2
ABCD2
CLCA4
FKBP1B
RAB11FIP2
ABCF1
ATP10B
PSME4
ATP11B
PMPCA
ATP11A
NEDD4L
ATP13A2
ABCB10
ABCB9
ABCA6
ABCA5
CES3
LRRC8B
ATP6V0A2
SGK3
ABCA4
ATP6V0D2
ATP6V1C2
FTH1
FTL
MCOLN2
PCSK9
NALCN
LDLRAP1
TRPC4AP
ABCA12
STEAP2
FBXL5
BEST4
ATP2C1
ERLEC1
ANGPTL3
GNAS
GNB1
GNB2
GNB3
GNG3
GNG4
GNG5
GNG7
GNG10
GNG11
GNGT1
GNGT2
AQP11
SLC9C2
UNC80
SLC9C1
MICU3
ATP11C
OSTM1
FLVCR1
MYLIP
ZDHHC8
TRPM5
HBA1
HBA2
HBB
HDLBP
HFE
STOML2
HMOX1
HMOX2
APOF
APOA1
APOA2
APOA4
APOB
GPIHBP1
ANO9
ABCB5
APOC1
AQP8
APOC2
ATP13A5
APOC3
APOC4
APOE
NIPAL4
AQP1
AQP2
AQP3
AQP4
AQP5
AQP6
AQP7
IREB2
AQP9
ABCC6
ATP9B
AQP12A
KCNJ11
LCAT
LCN2
LDLR
LETM1
LIPA
LIPC
ASIC2
LPA
LPL
ASIC1
MB
MIP
TRPM1
ABCC1
ASPH
MTTP
MYO5B
NEDD8
ATP1A1
ATP1A2
ATP1A3
ATP12A
ACO1
ATP1A4
ATP1B1
ATP1B2
ATP1B3
FXYD2
NPC1
ATP2A1
ATP2A2
ATP2A3
ATP2B1
ATP2B2
ATP2B3
ATP2B4
ATP4A
ATP4B
P4HB
FURIN
PCSK6
ATP6V0A4
ANO7
DERL2
CUTC
SAR1B
ANGPTL4
CYB5R4
PCSK5
SLC22A17
MBTPS2
ATP6V1D
TRPV2
LSR
ATP6V1H
CYB5R2
CYB5R1
ATP8A2
GNG13
ASIC5
ATP8B1
ATP6V1A
ABCB1
ABCB4
PHB1
ATP6V1B1
ATP6V1B2
ATP6V0C
ATP6V1C1
ATP6V1E1
PIP
ATP6V0B
TPCN1
ATP6V1G2
FXYD1
FXYD3
ATP6V0A1
PLN
PLTP
ATP6AP1
ATP7A
FXYD7
FXYD6
FXYD4
ATP7B
GNG2
TRPM4
TRPM7
BEST2
SLC66A1
MCUB
ANO1
ANO10
LRRC8D
STEAP3
MCOLN3
AVPR2
PARL
TRPV6
ASIC4
PRKACA
PRKACB
PRKACG
PRKAR1A
PRKAR1B
PRKAR2A
PRKAR2B
CAND1
ANGPTL8
APOBR
GNG12
ANKH
LRRC8A
AZGP1
TRPV5
PSMA1
PSMA2
PSMA3
PSMA4
PSMA5
PSMA6
PSMA7
PSMB1
PSMB2
PSMB3
PSMB4
PSMB5
PSMB6
PSMB7
PSMB8
PSMB9
PSMB10
PSMC1
PSMC2
PSMC3
PSMC4
PSMC5
PSMC6
PSMD1
PSMD2
PSMD3
PSMD4
ANO2
PSMD5
TRPC7
PSMD7
ATP13A1
PSMD8
PSMD9
PSMD10
PSMD11
PSMD12
NIPAL3
PSMD13
MCOLN1
ATP10A
ATP8B2
PSME1
ATP10D
PSME2
TTYH1
MRS2
NCEH1
UNC79
ANO8
NGB
PEX19
ABCD3
RAF1
TRPV4
GNB4
RNF5
CYB5RL
RPS27A
RYR1
RYR2
RYR3
SCNN1A
SCNN1B
SCNN1D
SCNN1G
CIDEC
ANO3
SEL1L
ABCG4
ABCG5
ABCG8
SGK1
LMF1
BMP1
SKP1
WNK1
WNK4
WNK3
WNK2
SLN
SOAT1
SPG7
TF
TFR2
TFRC
TRPC1
TRPC3
TRPC4
TRPC5
TRPC6
TRPM2
UBA52
UBB
UBC
NR1H2
VCP
VDAC1
VDAC2
VDAC3
VLDLR
BEST1
TRPV1
CA1
CA2
CA4
BSND
TRPM8
DERL1
MAIP1
SEM1
NIPAL2
ATP8B4
CYBRD1
TUSC3
TRPM3
LRRC8E
CUBN
TTYH3
CAMK2A
CAMK2B
NIPA2
AKAP1
AMN
CAMK2D
CAMK2G
MAGT1
LRRC8C
ATP13A4
SOAT2
CASQ1
CASQ2
CUL1
CREB3L3
PEX3
ABCC11
ABCC3
MBTPS1
RIPK1
RAB11A
EIF2S2
ABCC10
AQP10
TRPA1
ATP6V0E1
ATP6V1E2
MCU
ATP6V0D1
LMF2
DERL3
RNF185
SMDT1
ATP6V1F
ASIC3
MMGT1
LIPG
TTYH2
FTMT
GNG8
ABCG2
SCARB1
PSMF1
PMPCB
ATP6V1G1
ABCG1
CLCA2
PSMD6
ATP2C2
*Darkness represents the genes rank within the SuperPath, via the multiplicity of each gene in the constituent pathways.
STRING interaction network
for
Transport of inorganic cations/anions and amino acids/oligopeptides
SuperPath